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rs796052665

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GC;GC) 0 common in clinvar
Make rs796052665(AA;AA)
Make rs796052665(AA;GC)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63413478
GeneKCNQ2, LOC105372724
is asnp
is mentioned by
dbSNPrs796052665
dbSNP (old)rs796052665
ClinGenrs796052665
ebirs796052665
HLIrs796052665
Exacrs796052665
Gnomadrs796052665
Varsomers796052665
Maprs796052665
PheGenIrs796052665
Biobankrs796052665
1000 genomesrs796052665
hgdprs796052665
ensemblrs796052665
gopubmedrs796052665
geneviewrs796052665
scholarrs796052665
googlers796052665
pharmgkbrs796052665
gwascentralrs796052665
openSNPrs796052665
23andMers796052665
23andMe allrs796052665
SNP Nexus

SNPshotrs796052665
SNPdbers796052665
MSV3drs796052665
GWAS Ctlgrs796052665
Max Magnitude0
ClinVar
Risk rs796052665(AA;AA)
Alt rs796052665(AA;AA)
Reference Rs796052665(GC;GC)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62044831_62044832delGCinsTT
CLNSRC
CLNACC RCV000187944.1,